RESUMEN
We recently introduced a novel, to the best of our knowledge, infrared laser ellipsometer for sub-decisecond spectroscopy [Opt. Lett.44, 4387 (2019)10.1364/OL.44.004387] and 0.03 mm2 spot-sized hyperspectral imaging [Opt. Lett.44, 4893 (2019)10.1364/OL.44.004893]. Here we report on the next device generation for thin-film sensitive simultaneous single-shot amplitude and phase measurements. The multi-timescale ellipsometer achieves 10 µs time resolution and long-term stability over hours at high spectral resolution (0.2 cm-1). We investigate the temporal stages (from minutes to milliseconds) of fatty acid thin-film formation upon solvent evaporation from acetone-diluted microliter droplets. Optical thickness variations, structure modifications, and molecular interactions are probed during the liquid-to-solid phase transition. Multi-timescale ellipsometry could greatly impact fields like in situ biosensing, microfluidics, and polymer analytics, but also operando applications in membrane research, catalysis, and studies of interface processes and surface reactions.
RESUMEN
Dysregulation of extracellular signal-regulated kinases (ERK1/2) is linked to several diseases including heart failure, genetic syndromes and cancer. Inhibition of ERK1/2, however, can cause severe cardiac side-effects, precluding its wide therapeutic application. ERKT188-autophosphorylation was identified to cause pathological cardiac hypertrophy. Here we report that interference with ERK-dimerization, a prerequisite for ERKT188-phosphorylation, minimizes cardiac hypertrophy without inducing cardiac adverse effects: an ERK-dimerization inhibitory peptide (EDI) prevents ERKT188-phosphorylation, nuclear ERK1/2-signaling and cardiomyocyte hypertrophy, protecting from pressure-overload-induced heart failure in mice whilst preserving ERK1/2-activity and cytosolic survival signaling. We also examine this alternative ERK1/2-targeting strategy in cancer: indeed, ERKT188-phosphorylation is strongly upregulated in cancer and EDI efficiently suppresses cancer cell proliferation without causing cardiotoxicity. This powerful cardio-safe strategy of interfering with ERK-dimerization thus combats pathological ERK1/2-signaling in heart and cancer, and may potentially expand therapeutic options for ERK1/2-related diseases, such as heart failure and genetic syndromes.
Asunto(s)
Cardiotoxicidad , Péptidos de Penetración Celular/farmacología , Dimerización , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Sistema de Señalización de MAP Quinasas , Animales , Técnicas de Cultivo de Célula , Péptidos de Penetración Celular/síntesis química , Péptidos de Penetración Celular/toxicidad , Neoplasias del Colon/tratamiento farmacológico , Neoplasias del Colon/metabolismo , Sistemas de Liberación de Medicamentos , Quinasas MAP Reguladas por Señal Extracelular/efectos de los fármacos , Insuficiencia Cardíaca/tratamiento farmacológico , Insuficiencia Cardíaca/metabolismo , Humanos , Neoplasias Pulmonares/tratamiento farmacológico , Neoplasias Pulmonares/metabolismo , Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Sistema de Señalización de MAP Quinasas/fisiología , Ratones , Ratones Endogámicos C57BL , Medicina Molecular , Ratas , Ratas Sprague-Dawley , Transducción de SeñalRESUMEN
In situ mid-infrared (MIR) spectroscopy in liquids is an emerging field for the analysis of functional surfaces and chemical reactions. Different basic geometries exist for in situ MIR spectroscopy in milliliter (mL) and microfluidic flow cells, such as attenuated total reflection (ATR), simple reflection, transmission and fiber waveguides. After a general introduction of linear optical in situ MIR techniques, the methodology of ATR, ellipsometric and microfluidic applications in single-reflection geometries is presented. Selected examples focusing on thin layers relevant to optical, electronical, polymer, biomedical, sensing and silicon technology are discussed. The development of an optofluidic platform translates IR spectroscopy to the world of micro- and nanofluidics. With the implementation of SEIRA (surface enhanced infrared absorption) interfaces, the sensitivity of optofluidic analyses of biomolecules can be improved significantly. A large variety of enhancement surfaces ranging from tailored nanostructures to metal-island film substrates are promising for this purpose. Meanwhile, time-resolved studies, such as sub-monolayer formation of organic molecules in nL volumes, become available in microscopic or laser-based set-ups. With the adaption of modern brilliant IR sources, such as tunable and broadband IR lasers as well as frequency comb sources, possible applications of far-field IR spectroscopy in in situ sensing with high lateral (sub-mm) and time (sub-s) resolution are considerably extended.
RESUMEN
We recently presented a novel laser-based infrared (IR) spectroscopic phase-amplitude polarimeter for sub-decisecond and sub-mm2 measurements of organic thin films [Opt. Lett.44, 4387 (2019)OPLEDP0146-959210.1364/OL.44.004387]. Here we report on the hyperspectral-imaging capabilities of this device. The single-shot polarimeter employs a broadly tunable mid-IR (1318-1765 cm-1) quantum cascade laser (QCL) and a four-channel beam-division design for simultaneous phase and amplitude measurements. Fast QCL tuning speeds of up to 1500 cm-1/s enable hyperspectral mapping of large sample areas (50×50 mm2) within several tens of minutes, achieving 120 µm spatial and <0.5 cm-1 spectral resolution. We apply the instrument for imaging both the heterogeneous chemical and structural properties of sub-100 nm thin polymer and fatty-acid films. Our polarimeter opens up new applications regarding laterally resolved IR analyses of complex thin films.
RESUMEN
We report on the first, to the best of our knowledge, sub-second, sub-mm2 infrared (IR) spectroscopic measurements of thin organic films employing a laser-based phase-amplitude polarimeter in reflection geometry. The polarimeter uses a broadband mid-IR quantum cascade laser tunable between 1318 cm-1 and 1765 cm-1, as well as a single-shot beam division scheme for simultaneous single-pulse phase and amplitude measurements. The instrument achieves 120 µm spatial and <0.5 cm-1 spectral resolution, while providing unrivaled performance in terms of acquisition times. Spectral measurements within 100 ms and single-wavelength tracking at 16 µs are now possible. Investigating the vibrational properties accessible in the mid-IR, the polarimeter was applied for monitoring changes in molecular interactions of a 150 nm thin myristic acid film during its thermal phase transition around 55°C.
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In the last few decades, the use of plasmonics in vibrational spectroscopy has expanded the scope of (bio)analytical investigations. Nevertheless, there is a demand for a combined platform that can be simultaneously efficient for Surface Enhanced Raman Scattering (SERS) and Surface Enhanced Infrared Absorption (SEIRA). Here, we present a solution on the basis of a plasmonic Ag nanoparticle layer with a thickness gradient. The optical resonance along the layer varies from the visible to the infrared range offering optimal and intermediate sites for SERS and SEIRA of the analyte molecule (mercaptobenzonitrile). Enhancement factors for the same mode were determined to be ca. 104 and 170 for SERS and SEIRA, respectively. We present a full optical and vibrational characterization and demonstrate further tunability. The platform resolves reproducibility and comparability issues by a combination of the two methods. It also offers individualized solutions for different investigation conditions, i.e. a choice between excitation wavelengths and resonant Raman molecules. The multiple applicabilities of the presented unifying substrate can contribute to the expansion of the vibrational spectroscopic field and to analytics.
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Nondestructive label-free bioanalytics of microliter to nanoliter sample volumes with low analyte concentrations requires novel analytic approaches. For this purpose, we present an optofluidic platform that combines surface-enhanced in situ infrared spectroscopy with microfluidics for sensing of surface-immobilized ultrathin biomolecular films in liquid analytes. Submonolayer sensitivity down to surface densities of few ng/cm2 is demonstrated for the adsorption of the thiolate tripeptide glutathione and for the recognition of streptavidin on a biotinylated enhancement substrate. Nonfunctionalized and functionalized metal island films on planar oxidized silicon substrates are used for signal enhancement with quantifiable enhancement properties. A single-reflection geometry at an incidence angle below the attenuated-total-reflection (ATR) regime is used with ordinary planar, IR-transparent windows. The geometry circumvents the strong IR absorption of common polymer materials and of aqueous environments in the IR fingerprint region. This practice enables straightforward quantitative analyses of, e.g., adsorption kinetics as well as chemical and structural properties in dependence of external stimuli.
Asunto(s)
Técnicas Biosensibles/métodos , Técnicas Analíticas Microfluídicas/métodos , Nanotecnología/métodos , Espectrofotometría Infrarroja/métodos , Adsorción , Glutatión/química , Oro/química , Siliconas/química , Estreptavidina/análisisRESUMEN
We report a novel route for the functionalization of any substrates, including chemically inert substrates. CVD grown graphene is electrochemically functionalized with p-(N-maleimido)phenyl residues and consecutively transferred to various substrates. The transfer process is shown to be without noticeable loss. The functional layer exhibits a thickness of appx. 4.5 nm.